Canonical Allele Identifier: CA399966655
Gene: NOG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.56594807C>T , CM000679.2:g.56594807C>T GRCh38
NC_000017.10:g.54672168C>T , CM000679.1:g.54672168C>T GRCh37
NC_000017.9:g.52027167C>T NCBI36
NG_011958.1:g.6109C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000332822.6:c.584C>T MANE Select ENSP00000328181.4:p.Ser195Phe
ENST00000332822.4:c.584C>T ENSP00000328181.4:p.Ser195Phe
NM_005450.4:c.584C>T NP_005441.1:p.Ser195Phe
NM_005450.6:c.584C>T MANE Select NP_005441.1:p.Ser195Phe